DeRoyal Industries recalls ACDF Pack model REF 89-8779.03 due to potential injury from improper use. Affected units have specific lot numbers and expiration dates.
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DeRoyal Industries is recalling ACDF Pack model REF 89-8779.03 because it may cause injury if used improperly. This recall affects specific lot numbers with expiration dates listed in the notice.
The hazard is not clearly described in the recall notice. Without specific details about how the product could cause injury, it's impossible to explain the hazard mechanism.
This recall affects individuals who purchased the DeRoyal ACDF Pack with lot numbers 56188891 (expires Dec 1, 2023) or 56675066 (expires Jul 1, 2023). Patients using this product for spinal fusion surgery are most at risk.
Check your DeRoyal ACDF Pack for lot numbers 56188891 (expires Dec 1, 2023) or 56675066 (expires Jul 1, 2023). The product is used in spinal fusion surgery.
Look for lot numbers 56188891 (expires Dec 1, 2023) or 56675066 (expires Jul 1, 2023) on the packaging.
The recall notice does not specify the hazard mechanism.
Check for lot numbers 56188891 (expires Dec 1, 2023) or 56675066 (expires Jul 1, 2023).
The recall notice does not provide a remedy or action steps beyond checking the lot number.
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-0625-2023 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-0625-2023 from DeRoyal. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
